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Essentials of European Regulatory Affairs (Online Course)
The Organisation for Professionals in Regulatory Affairs
The world of Regulatory Affairs can be a confusing and complex place, particularly if you have no formal industry background....
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Professional Training
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From 340 GBP
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Online
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Self-Paced Online
Pharmaceutical Regulatory Affairs in China
PTI
Develop or market your drug in China more effectively with a deep understanding of the Chinese pharmaceutical regulatory landscape. In...
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Professional Training
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From 1,200 GBP
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Online
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Virtual Classroom
Pharmaceutical Regulatory Affairs in Asia
4.1
(14)
International Professional & Industry Academy
The pharmaceutical market in Asia is growing at a rapid pace and presents both opportunities and challenges to those wishing...
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Professional Training
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3 days
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From 1,349 GBP
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Online
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Virtual Classroom
Regulatory Guide to the Generics Market
PTI
Bringing a generic drug to market can be fraught with regulatory challenges and compliance issues. Alongside the high amount of...
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Professional Training
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3 weeks
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From 810 GBP
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Online
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Self-Paced Online
Pharmaceutical Regulatory Affairs in the Middle East
4.3
(21)
International Professional & Industry Academy
This seminar will provide you with an essential overview of the key areas of pharmaceutical regulatory affairs in the Middle...
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Professional Training
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2 days
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From 1,099 GBP
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Online
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Virtual Classroom
Introduction to EU Regulatory Affairs
5.0
(5)
PTI
This introductory course will provide you with a grounding knowledge of regulatory affairs in Europe. After three days you will...
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Professional Training
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From 1,200 GBP
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Online
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Virtual Classroom
Pharmaceutical Regulatory Affairs in Africa
4.6
(7)
International Professional & Industry Academy
The value of the African pharmaceutical market is increasing and growth is expected to continue at a rapid pace. There...
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Professional Training
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2 days
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From 1,099 GBP
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Online
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Virtual Classroom
Fundamentals of the EU IVD Regulation
PTI
The in-vitro diagnostic sector has undergone a regulatory transformation, similar to that seen in medical devices. Under the existing Directive,...
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Professional Training
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5 weeks
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From 999 GBP
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Online
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Self-Paced Online
Fundamentals of European Regulatory Affairs
4.8
(11)
PTI
This course is designed to guide RA professionals through the necessary regulatory skills and understanding for optimising drug submission procedures....
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Professional Training
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3 days
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From 1,895 GBP
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London
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Classroom
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Beginner level
Optimising Regulatory Strategies for Orphan Drugs
The Organisation for Professionals in Regulatory Affairs
This CRED course will provide a comprehensive understanding of the opportunities and challenges offered by orphan drug regulations and practical...
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Professional Training
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1 day
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From 675 GBP
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Online
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Self-Paced Online
Post Market Surveillance and Vigilance Requirements for Manufacturers (EU 2017/745)
NSF International, Health Sciences
Post-market surveillance for manufacturers is covered in Articles 83-86. Articles 87-89 cover post-market vigilance requirements. This course reviews the requirements...
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Professional Training
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1 hour
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From 299 USD
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Online
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Self-Paced Online
Introduction to the In-Vitro Diagnostic Regulation (IVDR)
4.7
(6)
International Professional & Industry Academy
The In-Vitro Diagnostic Regulation (EU) 2017/746, which came into force in May 2017 with a transition period of five years,...
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Professional Training
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2 days
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From 1,099 GBP
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Online
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Virtual Classroom
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Beginner level
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